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Degradation of ribonucleic acid by immobilized ribonuclease
Author(s) -
Dale Bruce E.,
White Don H.
Publication year - 1979
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.260210910
Subject(s) - ribonuclease , degradation (telecommunications) , chemistry , biochemistry , rna , chromatography , telecommunications , computer science , gene
An immobilized enzyme (pancreatic ribonuclease bound to porous titania) was investigated for the degradation of purified yeast ribonucleic acid as a substrate. The immobilized enzyme is active and stable in the pH range 4–8. Dependence of enzymatic activity on ionic strength, pH, temperature, fluid flow rate, and substrate concentration were investigated. A cummulative fluid residence time of 6 sec is sufficient for 5% substrate conversion at 25°C and pH 7.0. The critical flow rate (i.e., the fluid flow rate necessary to remove film diffusion resistance) approximately doubles with each 10°C rise in reaction temperature. The critical flow rates obtained in this study are about 40 times greater than those obtained for a similar study on immobilized glucose oxidase. Arrhenius plots gave activation energies of −9.6 and −7.1 kcal/g mol at pH 4.6 and 7.0, respectively. The work reported herein is a bench‐scale investigation of an immobilized enzyme with primary emphasis on the mass transfer and kinetic characteristics of the system. The rapid reaction rates obtainable at relatively low temperatures offfer a potential alternative method of purifying yeast single cell protein (SCP) with minimum loss of desired protein. The key questions are how such a system would react in a yeast homogenate, what conditions in such a system must be controlled, and what type of immobilized reactor should be utilized, if such further work continued to show promise.